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The Intellectual Property Office offers different methods of accelerating the processing of your patent application.
Check how much your visa application costs in the country you’re in
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
The family procedure rules are a single set of rules governing the practice and procedure in family proceedings in the high court, county courts and magistrates' courts.
Listing of countries with a known occurrence of high consequence infectious disease (HCID).
When tests to detect COVID-19 are commonly used (use cases) and what to consider when deciding which type of test to employ.
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
Protocols and procedures for testing the distinctiveness, uniformity and stability (DUS) of certain agricultural and vegetable plants.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Class and permitted use of passenger ships, cargo ships, tankers, tugs, tenders, fishing boats, yachts, commercial vessels, and the required certificates.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
Find schemes that have told HMRC they meet the conditions to be a recognised overseas pension scheme (ROPS).
Goods that are controlled and how to get licences for them, the UK Strategic Export Control Lists, dealing with the Export Control Organisation (ECO).
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
The UK Good Laboratory Practice Monitoring Authority (UK GLPMA) recognises that there are potential challenges COVID-19 will present to members of the GLP monitoring programme.
The MHRA is part of the Access Consortium along with the Therapeutic Goods Administration, Health Canada, Health Sciences Authority of Singapore and Swissmedic.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
This guidance specifies the standards for the continuous monitoring and sampling of stack emissions.
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
Don’t include personal or financial information like your National Insurance number or credit card details.
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